Drug for reducing side effects of leflunomide
A technology for side effects and fomit, which is applied in the field of medicines to reduce the side effects of levomide, can solve the problems of elevated liver enzymes, affecting treatment, and reducing the quality of life of patients
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Embodiment approach 1
[0009] Embodiment 1: The drug for reducing the side effects of Leformide consists of 10 parts of Leformide, 40 parts of microcrystalline cellulose, 30 parts of starch, 3 parts of polyethylene glycol, 1 part of magnesium stearate, 6 parts of biological preparations, Made from 4 parts of sodium lauryl sulfate and 30 parts of hydroxypropyl cellulose. Pulverize leflunomide and biological preparations, weigh leflunomide, biological preparations, microcrystalline cellulose, starch, sodium lauryl sulfate, and polyethylene glycol and mix well, then add 8% hydroxypropyl Appropriate amount of cellulose aqueous solution, made into soft material, granulated, air-dried, granulated, added with prescribed amount of magnesium stearate, mixed evenly, compressed into tablets, ready to be obtained. Described polyethylene glycol is polyethylene glycol 4000. The biomass powder is mixed and pulverized by 20 parts of Xiangmu Jungui, 80 parts of Huangsuo Meigen, and 15 parts of Centella asiatica, ad...
Embodiment approach 2
[0010] Embodiment 2: The drug for reducing the side effects of Leformide consists of 14 parts of Leformide, 50 parts of microcrystalline cellulose, 40 parts of starch, 6 parts of polyethylene glycol, 3 parts of magnesium stearate, 10 parts of biological preparations, Made from 6 parts of sodium lauryl sulfate and 36 parts of hydroxypropyl cellulose, the preparation method is the same as the first embodiment.
Embodiment approach 3
[0011] Embodiment 3: The drug for reducing the side effects of Leformide consists of 12 parts of Leformide, 45 parts of microcrystalline cellulose, 35 parts of starch, 4 parts of polyethylene glycol, 2 parts of magnesium stearate, 8 parts of biological preparations, It is prepared by 5 parts of sodium lauryl sulfate and 33 parts of hydroxypropyl cellulose, and the preparation method is the same as the first embodiment.
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